KENDALL T.E.D./SCD SEQUENTIAL COMPRESSION DEVICE
FDA 510(k) clearance K932835 · decided 1993-08-06
Clearance details
- K-number
- K932835
- Device name
- KENDALL T.E.D./SCD SEQUENTIAL COMPRESSION DEVICE
- Applicant
- Kendall Healthcare Products Co. Div.Of Tyco Health
- Decision
- Substantially Equivalent
- Date received
- 1993-06-10
- Decision date
- 1993-08-06
- Days to decision
- 57 days
- Clearance type
- Traditional
- Product code
- JOW
- Device class
- 2
- Regulation number
- 870.5800
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Mansfield, MA, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
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Recalls involving this device
No recalls on record reference this clearance.